We are looking for a Clinical Evidence Specialist – Literature Review to join our Product Research Team.

In this role, you will apply your scientific training to literature review, evidence interpretation, and clinical evidence documentation for Nox Medical products. The work is primarily focused on gathering, reviewing and evaluating scientific literature and clinical data to support regulatory clinical evaluation, post market clinical follow-up (PMCF), and clinical validation documentation.

You will plan and document literature searches, extract and summarize relevant evidence, interpret the state of the art, and help translate scientific findings into clear, traceable documentation. You will work closely with experienced colleagues in clinical evaluation, product research, quality, regulatory affairs, and product development.

This is a good opportunity for someone with a background in public health, life sciences, medicine, engineering, biostatistics, health economics, epidemiology, or a related scientific field who wants to apply literature and data interpretation skills in a regulated medical device environment.

The role covers Nox Medical’s Class I and Class IIa medical devices, including hardware, software (incl. AI-enabled functionality), and sensors, across global regulated markets, with particular focus on clinical evidence to meet the requirements of key regulatory frameworks such as the EU MDR, FDA, and TGA.

What You’ll Do

As a Clinical Evidence Specialist – Literature Review, your key responsibilities include:

• Plan, perform, and document structured literature searches related to Nox Medical products, similar or equivalent devices, clinical background, safety, performance, and the state of the art.
• Extract, summarize, and interpret relevant evidence from scientific publications, clinical guidelines, standards, and other sources.
• Prepare literature search protocols, literature search reports, evidence tables, and literature summaries in accordance with internal procedures and regulatory expectations.
• Critically appraise clinical evidence for relevance, quality, limitations, and applicability to Nox Medical products.
• Help define and document clinical performance and safety criteria based on state of the art literature, device risk profile, clinical expectations,  to align with product requirements and clinical claims.
• Contribute to clinical evaluation and clinical validation documentation, including background rationale, methods descriptions, endpoint selection, performance criteria, and interpretation of results.
• Work with colleagues to ensure that literature-based conclusions are scientifically sound, clearly written, traceable, and suitable for regulatory review.

What You Bring:
Education and Experience

• Master’s degree or PhD in Life Sciences, Medicine, Engineering, Biostatistics, Health Economics, Public Health, Epidemiology, Psychology, Neuroscience, or a related scientific discipline, or equivalent experience.
• Experience working with scientific or clinical literature, including reading, interpreting, appraising and synthesising evidence.
• Experience with structured literature searches, evidence extraction, systematic review methods, or medical writing is advantageous.
• Good understanding of clinical research methods, study design, data and statistics.
• Strong scientific writing skills and excellent command of written English.
• Experience with medical device clinical evaluation, clinical validation, regulatory documentation, or post-market clinical follow-up is a plus, but not required.
• Familiarity with literature databases such as PubMed or Embase, and reference management tools such as Zotero or EndNote, is advantageous.
• Experience in sleep medicine, respiratory physiology, biomedical signals, software as a medical device, AI-enabled medical devices, or sensor-based technologies is advantageous.

Personal and Professional Skills

• Analytical and detail-oriented, with the ability to assess the relevance and quality of scientific evidence.
• Structured and careful in documentation, traceability, and following procedures.
• Able to explain scientific findings clearly to both technical and non-technical colleagues.
• Comfortable working in a regulated environment with templates, SOPs, and controlled documents.
• Interested in medical device clinical evaluation, regulatory evidence requirements, and sleep diagnostics.
• Collaborative and pragmatic, with an interest in applying scientific evidence to real-world medical device development.

Why Join Nox Medical

At Nox Medical, you’ll join a multidisciplinary team working to advance sleep diagnostics and support better patient care.

You will play an important role in ensuring that our medical devices are supported by clear, traceable, and scientifically grounded clinical evidence documentation. Your work will help connect scientific literature, clinical data, product claims, and regulatory requirements.

This is a role for someone who enjoys working with scientific evidence and wants to apply those skills in an industry setting, where the output has a direct impact on medical device development, compliance, and patient care.